Drug application
NAFCILLIN SODIUM (NAFCILLIN SODIUM)
Drugs@FDA ANDA 091613 · EUGIA PHARMA SPECLTS
Key facts
| Drug name | NAFCILLIN SODIUM |
|---|---|
| Active ingredients | NAFCILLIN SODIUM |
| Application type | ANDA |
| Application number | 091613 |
| Company | EUGIA PHARMA SPECLTS |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | EQ 1GM BASE/VIAL |
| Marketing status | Prescription |
| TE codes | AP |
| Reference listed drug | No |
| Latest submission status date | Dec 26, 2012 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.